{
    "disease_id": "DOID:0111121",
    "recommended_name": {
        "id": "DOID:0111121",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111121",
        "name": "nephronophthisis 13",
        "description": "A nephronophthisis that has_material_basis_in homozygous or compound heterozygous mutation in the WDR19 gene on chromosome 4p14."
    },
    "synonyms": [
        {
            "id": "DOID:0111121",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111121",
            "name": "NPHP13",
            "description": ""
        },
        {
            "id": "MONDO:0013718",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013718",
            "name": "nephronophthisis 13",
            "description": "A nephronophthisis that has material basis in homozygous or compound heterozygous mutation in the WDR19 gene on chromosome 4p14."
        },
        {
            "id": "MONDO:0013718",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013718",
            "name": "NPHP13",
            "description": ""
        },
        {
            "id": "MONDO:0013718",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013718",
            "name": "nephronophthisis 13",
            "description": ""
        },
        {
            "id": "MONDO:0013718",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013718",
            "name": "nephronophthisis type 13",
            "description": ""
        },
        {
            "id": "MIM:614377",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614377",
            "name": "Nephronophthisis 13",
            "description": "Nephronophthisis 13"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111121"
    ],
    "unlinked_id_list": []
}